Clinical project manager previous regional & global experience - homebased - mex
updated: march 25, 2026
location: tlalnepantla, mex, mexico
job id:25106855
description
syneos health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
our clinical solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
whether you join us in a functional service provider partnership or a full‑service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
job responsibilities
* project leadership and delivery: manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with gcp, relevant sop’s, and regulatory requirements.
* acts as a primary liaison between the company and the customer to ensure timely study launch, conduct, and closeout according to the customer’s and the company’s contractual agreement.
* lead project team to ensure quality, timelines and budget management.
* accountable for the financial performance of each project; coordinates activities and deliverables of all study conduct partners and proactively identifies and manages issues.
* ensures studies are conducted in compliance with gcp, relevant sop’s and regulatory requirements; accountable for all project deliverables.
* responsible for the quality and completeness of tmf for assigned projects.
* accountable for maintenance of study information on a variety of databases and systems.
* responsible for study management components of inspection readiness for all aspects of the study conduct; oversight for development and implementation of project plans.
* plan, coordinate and present at internal and external meetings; prepare project management reports for clients and management.
* develop contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
* develops strong relationships with current clients to generate new and/or add‑on business for the future.
* may participate in bid defense meetings where presented as potential project manager.
* may be required to line‑manage other project management team members and clinical monitoring staff.
qualifications
* bachelor’s degree (or equivalent) in life sciences, medicine, pharmacy, nursing or equivalent combination of education and experience.
* clinical research organization (cro) experience and relevant therapeutic experience preferred; strong knowledge of good clinical practice/ich guidelines and other applicable regulatory requirements.
* strong organizational skills.
* ability to manage time and work independently.
* direct therapeutic area expertise.
* ability to embrace new technologies.
* excellent communication, presentation, interpersonal skills, both written and spoken.
* ability to travel as necessary (approximately 25%).
additional information
tasks, duties, and responsibilities as listed in this job description are not exhaustive. The company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the job description. The company, at its sole discretion, will determine what constitutes equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the eu equality directive, in relation to the recruitment and employment of its employees. The company is committed to compliance with the americans with disabilities act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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